LncRNA MYLK反义RNA 1通过microRNA-101-5p激活细胞分裂周期42/中性Wiskott-Aldrich综合征蛋白通路,加速结肠癌细胞上皮向间质转化。

The Kaohsiung journal of medical sciences Pub Date : 2024-01-01 Epub Date: 2023-11-11 DOI:10.1002/kjm2.12773
Zhen-Hao Quan, Fei-Peng Xu, Zhe Huang, Ri-Hong Chen, Qing-Wen Xu, Lin Lin
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摘要

长链非编码RNA MYLK反义RNA 1 (MYLK- as1)是多种疾病的关键。因此,本研究的目的是探讨MYLK-AS1的可能机制。收集62例结肠癌(CC)标本及配对的邻近正常组织,检测mylb - as1、microRNA (miR)-101-5p/细胞分裂周期42 (CDC42)的表达。用mylb - as1、miR-101-5p、cdc42相关质粒转染CC细胞系,分析细胞上皮间质转化(epithelial-mesenchymal transition, EMT)的生物学功能和标志物。评估MYLK-AS1、miR-101-5p和CDC42之间的结合关系。在CC组织和细胞系中,MYLK-AS1和CDC42高表达,miR-101-5p低表达。抑制MYLK-AS1或上调miR-101-5p可抑制CC细胞生长和EMT。miR-101-5p通过靶向CDC42抑制CC细胞中CDC42/N-wasp轴的激活。CDC42的敲低或miR-101-5p的上调部分逆转了mylar - as1上调引起的影响。在CC中显著上调的myk - as1可能是miR-101-5p的分子海绵,myk - as1通过miR-101-5p靶向CDC42,促进CC细胞中CDC42/N-wasp轴的激活,进而促进肿瘤的发展。MYLK-AS1可能是CC治疗的潜在生物标志物和靶点。
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LncRNA MYLK antisense RNA 1 activates cell division cycle 42/Neutal Wiskott-Aldrich syndrome protein pathway via microRNA-101-5p to accelerate epithelial-to-mesenchymal transition of colon cancer cells.

Long noncoding RNA MYLK antisense RNA 1 (MYLK-AS1) is the crux in multiple diseases. Therefore, the purpose of this study was to investigate the possible mechanism of MYLK-AS1. A total of 62 colon cancer (CC) specimens and paired adjacent normal tissues were collected, and the expression of MYLK-AS1, microRNA (miR)-101-5p/cell division cycle 42 (CDC42) was detected. CC cell lines were transfected with MYLK-AS1, miR-101-5p, CDC42-related plasmids, and the biological functions and markers of epithelial-mesenchymal transition (EMT) were analyzed. The binding relationship between MYLK-AS1, miR-101-5p, and CDC42 was evaluated. In CC tissues and cell lines, MYLK-AS1 and CDC42 were highly expressed, and miR-101-5p was lowly expressed. Inhibition of MYLK-AS1 or upregulation of miR-101-5p can inhibit CC cell growth and EMT. miR-101-5p inhibited CDC42/N-wasp axis activation in CC cells by targeting CDC42. Knockdown of CDC42 or upregulation of miR-101-5p partially reversed the effects caused by upregulation of MYLK-AS1. MYLK-AS1, which is significantly upregulated in CC, may be a molecular sponge for miR-101-5p, and MYLK-AS1 promotes the activation of the CDC42/N-wasp axis in CC cells by targeting CDC42 through miR-101-5p, which in turn promotes tumor development. MYLK-AS1 may be a potential biomarker and target for CC therapy.

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